BEUDAMED
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    MERIVAARA OBSTETRIC CHAIR/BED MODEL 358

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283792·

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124153·Modular Offset Stem 11mm x 75mm x 4mm

    Sniper Spine System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AquaCast Mask

    FDA 510(k)
    FDA Class 2 ·Radiology

    DRILL, AO T2 Ø3,5X130 MM

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HWE·August 23, 2024

    ACCOLADE TMZF FEMORAL RASP SIZE 4

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·June 5, 2014

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 4, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·November 12, 2012

    Dunlee DA 200 Ultra & MX 200 Ultra CT X-Ray Tube Housing Assembly (989600088701); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Dunlee DA 200 PRO & MX 200 PRO CT X-Ray Tube Housing Assembly (989600088401); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Dunlee DA 200 & MX 200 CT X-Ray Tube Housing Assembly (989600087501); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005